EU IDMP Implementation Guide – version 2.1

EMA released version 2.1 of the EU IDMP Implementation Guide (EU IG v2.1) in June 2021. It provides standardised definitions for the identification and description of medicinal products for human use. The new version supports the implementation of Product Management Service (PMS) Step 1 and data submission on medicinal products authorised under the centralised procedure.
_{July 5, 2021}